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Journal Abstract Search
165 related items for PubMed ID: 8568800
1. Structure-antigastrin activity relationships of new spiroglumide amido acid derivatives. Makovec F, Peris W, Frigerio S, Giovanetti R, Letari O, Mennuni L, Revel L. J Med Chem; 1996 Jan 05; 39(1):135-42. PubMed ID: 8568800 [Abstract] [Full Text] [Related]
2. Cytosolic Ca2+ evaluation in rabbit parietal cells: a novel method to screen gastrin receptor antagonists. Letari O, Mennuni L, Revel L, Colombo S, Makovec F. Eur J Pharmacol; 1996 Jun 13; 306(1-3):325-33. PubMed ID: 8813647 [Abstract] [Full Text] [Related]
3. Structure-antigastrin activity relationships of new (R)-4-benzamido-5-oxopentanoic acid derivatives. Makovec F, Peris W, Revel L, Giovanetti R, Mennuni L, Rovati LC. J Med Chem; 1992 Jan 13; 35(1):28-38. PubMed ID: 1732532 [Abstract] [Full Text] [Related]
4. Characterization of the binding of [3H]L-365,260: a new potent and selective brain cholecystokinin (CCK-B) and gastrin receptor antagonist radioligand. Chang RS, Chen TB, Bock MG, Freidinger RM, Chen R, Rosegay A, Lotti VJ. Mol Pharmacol; 1989 Jun 13; 35(6):803-8. PubMed ID: 2733696 [Abstract] [Full Text] [Related]
5. Characterization of antisecretory and antiulcer activity of CR 2945, a new potent and selective gastrin/CCK(B) receptor antagonist. Makovec F, Revel L, Letari O, Mennuni L, Impicciatore M. Eur J Pharmacol; 1999 Mar 12; 369(1):81-90. PubMed ID: 10204685 [Abstract] [Full Text] [Related]
6. Structure-based design of new constrained cyclic agonists of the cholecystokinin CCK-B receptor. Blommaert AG, Dhôtel H, Ducos B, Durieux C, Goudreau N, Bado A, Garbay C, Roques BP. J Med Chem; 1997 Feb 28; 40(5):647-58. PubMed ID: 9057851 [Abstract] [Full Text] [Related]
7. Biochemical and pharmacological profiles of loxiglumide, a novel cholecystokinin-A receptor antagonist. Fukamizu Y, Nakajima T, Kimura K, Kanda H, Fujii M, Saito T, Kasai H. Arzneimittelforschung; 1998 Jan 28; 48(1):58-64. PubMed ID: 9522034 [Abstract] [Full Text] [Related]
8. Effect of dexloxiglumide and spiroglumide, two new CCK-receptor antagonists, on gastric emptying and secretion in the rat: evaluation of their receptor selectivity in vivo. Scarpignato C, Kisfalvi I, D'Amato M, Varga G. Aliment Pharmacol Ther; 1996 Jun 28; 10(3):411-9. PubMed ID: 8791971 [Abstract] [Full Text] [Related]
9. RP 73870, a gastrin/cholecystokinin-B receptor antagonist with potent anti-ulcer activity in the rat. Pendley CE, Fitzpatrick LR, Capolino AJ, Davis MA, Esterline NJ, Jakubowska A, Bertrand P, Guyon C, Dubroeucq MC, Martin GE. J Pharmacol Exp Ther; 1995 Jun 28; 273(3):1015-22. PubMed ID: 7791071 [Abstract] [Full Text] [Related]
10. Pharmacological properties of ureido-acetamides, new potent and selective non-peptide CCKB/gastrin receptor antagonists. Bertrand P, Böhme GA, Durieux C, Guyon C, Capet M, Jeantaud B, Boudeau P, Ducos B, Pendley CE, Martin GE. Eur J Pharmacol; 1994 Sep 12; 262(3):233-45. PubMed ID: 7813588 [Abstract] [Full Text] [Related]
11. Pharmacological properties of lorglumide as a member of a new class of cholecystokinin antagonists. Makovec F, Bani M, Cereda R, Chisté R, Pacini MA, Revel L, Rovati LA, Rovati LC, Setnikar I. Arzneimittelforschung; 1987 Nov 12; 37(11):1265-8. PubMed ID: 3440035 [Abstract] [Full Text] [Related]
12. Peripheral biological activity of SR 27897: a new potent non-peptide antagonist of CCKA receptors. Gully D, Fréhel D, Marcy C, Spinazzé A, Lespy L, Neliat G, Maffrand JP, Le Fur G. Eur J Pharmacol; 1993 Feb 23; 232(1):13-9. PubMed ID: 7681406 [Abstract] [Full Text] [Related]
13. Lorglumide and loxiglumide inhibit gastrin-stimulated DNA synthesis in a rat tumoral acinar pancreatic cell line (AR42J). Seva C, Scemama JL, Bastié MJ, Pradayrol L, Vaysse N. Cancer Res; 1990 Sep 15; 50(18):5829-33. PubMed ID: 2393852 [Abstract] [Full Text] [Related]
14. Synthesis and stereochemical structure-activity relationships of 1,3-dioxoperhydropyrido[1,2-c]pyrimidine derivatives: potent and selective cholecystokinin-A receptor antagonists. Martín-Martínez M, Bartolomé-Nebreda JM, Gómez-Monterrey I, González-Muñiz R, García-López MT, Ballaz S, Barber A, Fortuño A, Del Río J, Herranz R. J Med Chem; 1997 Oct 10; 40(21):3402-7. PubMed ID: 9341915 [Abstract] [Full Text] [Related]
15. (3R)-N-(1-(tert-butylcarbonylmethyl)-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-3-yl)-N'-(3-(methylamino)phenyl)urea (YF476): a potent and orally active gastrin/CCK-B antagonist. Semple G, Ryder H, Rooker DP, Batt AR, Kendrick DA, Szelke M, Ohta M, Satoh M, Nishida A, Akuzawa S, Miyata K. J Med Chem; 1997 Jan 31; 40(3):331-41. PubMed ID: 9022799 [Abstract] [Full Text] [Related]
16. Receptor type for cholecystokinin on isolated intestinal muscle cells of the guinea pig. Morini G, Barocelli E, Impicciatore M, Grider JR, Makhlouf GM. Regul Pept; 1990 May 21; 28(3):313-21. PubMed ID: 2377745 [Abstract] [Full Text] [Related]
17. Pharmacological and biochemical evidence for the simultaneous expression of CCKB/gastrin and CCKA receptors in the pig pancreas. Philippe C, Lhoste EF, Dufresne M, Moroder L, Corring T, Fourmy D. Br J Pharmacol; 1997 Feb 21; 120(3):447-54. PubMed ID: 9031748 [Abstract] [Full Text] [Related]
18. Pharmacological characterisation of a new potent and specific nonpolypeptidic cholecystokinin antagonist. Setnikar I, Bani M, Cereda R, Chisté R, Makovec F, Pacini MA, Revel L, Rovati LC, Rovati LA. Arzneimittelforschung; 1987 Jun 21; 37(6):703-7. PubMed ID: 3663268 [Abstract] [Full Text] [Related]
19. Synthesis of phenoxyacetic acid derivatives as highly potent antagonists of gastrin/cholecystokinin-B receptors. II. Takeda Y, Kawagoe K, Yokomizo A, Yokomizo Y, Hosokami T, Shimoto Y, Tabuchi Y, Ogihara Y, Otsubo R, Honda Y, Yokohama S. Chem Pharm Bull (Tokyo); 1998 Jun 21; 46(6):951-61. PubMed ID: 9658573 [Abstract] [Full Text] [Related]
20. Different actions of CCK on pancreatic and gastric growth in the rat: effect of CCK(A) receptor blockade. Varga G, Kisfalvi K, Pelosini I, D'Amato M, Scarpignato C. Br J Pharmacol; 1998 Jun 21; 124(3):435-40. PubMed ID: 9647465 [Abstract] [Full Text] [Related] Page: [Next] [New Search]